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A Study of TORL-5-700 in Relapsed/Refractory Non Hodgkin's Lymphoma

RecruitingPhase 1/2

A Phase 1/2, First-in-Human, Open-Label, Multicenter Study of TORL-5-700 as a Monotherapy and in Combination for Participants With Relapsed or Refractory Non-Hodgkin Lymphoma

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Confirmed B-NHL, including but not limited to de novo DLBCL; FL, Grades 1 to 3A; MCL; transformed lymphoma (tFL, RT) and FL Grade 3B; MZL and MALT.
* Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to 2.
* At least 1 measurable lesion per Lugano criteria.
* Tumor tissue is available.
* Adequate organ function

Exclusion Criteria:

* T-cell lymphoma
* CLL or SL
* Burkitt lymphoma and high-grade B-cell lymphoma
* CNS involvement
* Peripheral neuropathy \> Grade 2
* Uncontrolled medical conditions
* Viral infections

About the study

A Phase 1/2 study to evaluate safety, tolerability, and anticancer activity of TORL-5-700 as a monotherapy and in combination in R/R NHL

What is being tested

Sponsor: TORL Biotherapeutics, LLC · Participants: 155 · Started: Mar 31, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07439653

Locations in the U.S.

CaliforniaProvidence Medical Foundation, Fullerton
Cancer and Blood Specialty Clinic, Los Alamitos, Los Alamitos
UCLA, Santa Monica
Stanford University, Stanford
FloridaUniversity of California Miami, Sylvester Comprehensive Cancer Center, Miami
IowaUniversity of Iowa Health Care, Iowa City
KansasCancer Center of Kansas, Wichita, Wichita
TennesseeSarah Cannon Research Institute, Nashville
TexasUniversity of Texas Southwestern Medical Center, Dallas

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.